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SAR407899

Catalog No. T7391 Copy Product Info
Purity: 99.42%
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SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.

SAR407899

Copy Product Info
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Catalog No. T7391

SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.

SAR407899
Cas No. 923359-38-0
Other Forms of SAR407899:
SAR407899 hydrochlorideT23308923262-96-8
In Stock
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Pack SizePriceUSA StockGlobal StockQuantity
2 mg$30In StockIn Stock
5 mg$48In StockIn Stock
10 mg$73In StockIn Stock
25 mg$137In StockIn Stock
50 mg$222In StockIn Stock
100 mg$355In StockIn Stock
200 mg$526In StockIn Stock
1 mL x 10 mM (in DMSO)$53In StockIn Stock
In stock · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Batch Information

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Purity:99.42%
Appearance:Solid
Color:White
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COA LCMS HNMR HPLC

Product Introduction

Bioactivity
Description
SAR407899 is Rho kinase inhibitor potently inhibits endothelin-1-induced constriction of renal resistance arteries.
Targets&IC50
ROCK1:276 nM (IC50), ROCK2:102 nM (IC50)
In vivo
In vivo, SAR407899 dose-dependently induced rabbit penile erection, with greater potency and longer duration of action than sildenafil[1].
Animal Research
Compared the effects of SAR407899, the Rho-kinase inhibitor Y-27632 and the PDE5 inhibitor sildenafil for their ability to relax corpus cavernosum strips contracted with phenylephrine in healthy and diabetic animals. Strips were obtained from WKY, spontaneous hypertensive (SHR), control CD, and diabetic CD rats, humans, control and diabetic rabbits. Diabetes was induced by streptozotocin or alloxan injection. In vivo penile erection (length) induced by drugs was measured in conscious rabbits[1].
Chemical Properties
Molecular Weight244.29
FormulaC14H16N2O2
Cas No.923359-38-0
SmilesO=c1[nH]ccc2cc(OC3CCNCC3)ccc12
Relative Density.1.193 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 6 mg/mL (24.56 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.0935 mL20.4675 mL40.9350 mL204.6748 mL
5 mM0.8187 mL4.0935 mL8.1870 mL40.9350 mL
10 mM0.4093 mL2.0467 mL4.0935 mL20.4675 mL
20 mM0.2047 mL1.0234 mL2.0467 mL10.2337 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

Keywords

SAR-407899SAR407899SAR 407899ROKROCKRho-kinaseRho-associated protein kinaseRho-associated kinaseRhoInhibitorinhibit
Related Tags: buy SAR407899 | purchase SAR407899 | SAR407899 cost | order SAR407899 | SAR407899 chemical structure | SAR407899 in vivo | SAR407899 formula | SAR407899 molecular weight
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